Canonical Allele Identifier: CA1153146160
Gene: KIF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10345774A= , CM000663.2:g.10345774A= GRCh38
NC_000001.10:g.10405832A= , CM000663.1:g.10405832A= GRCh37
NC_000001.9:g.10328419A= NCBI36
NG_008069.1:g.140069A= , LRG_252:g.140069A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696502.1:c.3752-71A= ENSP00000512668.1:n.3752-71A=
ENST00000696503.1:c.3614-71A= ENSP00000512669.1:n.3614-71A=
ENST00000696504.1:c.3614-71A= ENSP00000512670.1:n.3614-71A=
ENST00000676179.1:c.3689-71A= MANE Select ENSP00000502065.1:n.3689-71A=
ENST00000263934.10:c.3551-71A= ENSP00000263934.6:n.3551-71A=
ENST00000377081.5:c.3689-71A= ENSP00000366284.1:n.3689-71A=
ENST00000377086.5:c.3689-71A= ENSP00000366290.1:n.3689-71A=
ENST00000465635.5:n.144-71A=
ENST00000483340.1:n.154A=
ENST00000620295.2:c.3647-71A= ENSP00000478500.1:n.3647-71A=
ENST00000622724.3:c.3611-71A= ENSP00000480063.1:n.3611-71A=
NM_015074.3:c.3551-71A= , LRG_252t1:c.3551-71A= NP_055889.2:n.3551-71A=
NM_001365951.1:c.3689-71A= NP_001352880.1:n.3689-71A=
NM_001365952.1:c.3689-71A= NP_001352881.1:n.3689-71A=
NM_001365951.3:c.3689-71A= MANE Select NP_001352880.1:n.3689-71A=